Severe Arterial Forearm Thrombosis in an 11-year-old Girl with Homozygous Antithrombin Deficiency typ IIb Budapest 3 and Mild Factor VII Deficiency Due to Homozygous Polymorphisms in the Factor 7 Gene and Antithrombotic Treatment

B. Lohr,F. Verrel, C. Stuplich, A.C. Block,J. Oldenburg,B. Pötzsch,H.J. Hertfelder

Science meets clinical practiceHämostaseologie（2019）

引用 0|浏览0

暂无评分

摘要

Background: Inherited antithrombin (AT) type IIb Budapest 3 (AT Bp3) deficiency is a rare disorder affecting the heparin binding site of AT. Homozygosity for ATBp3 deficiency in contrast to a homozygous AT type I deficiency may not be fatal.

查看译文

关键词

homozygous antithrombin deficiency typ,mild factor vii deficiency,severe arterial forearm thrombosis,homozygous polymorphisms,year-old

AI 理解论文

溯源树

样例

生成溯源树，研究论文发展脉络

Chat Paper

正在生成论文摘要